Canonical Allele Identifier: CA378605574
Gene: HTRA1 HGNC NCBI

Linked Data

gnomAD v4: 10-122461778-G-T
MyVariant Identifiers: chr10:g.124221294G>T (hg19) chr10:g.122461778G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122461778G>T , CM000672.2:g.122461778G>T GRCh38
NC_000010.10:g.124221294G>T , CM000672.1:g.124221294G>T GRCh37
NC_000010.9:g.124211284G>T NCBI36
NG_011554.1:g.5254G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.126G>T MANE Select ENSP00000357980.3:p.Glu42Asp
ENST00000648167.1:c.154+3069G>T ENSP00000498033.1:n.154+3069G>T
ENST00000368984.7:c.126G>T ENSP00000357980.3:p.Glu42Asp
NM_002775.4:c.126G>T NP_002766.1:p.Glu42Asp
NM_002775.5:c.126G>T MANE Select NP_002766.1:p.Glu42Asp
Search 100 bp 5'
Search 100 bp 3'